Canonical Allele Identifier: CA203645080

Gene: ST8SIA6

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.17346144C>T , CM000672.2:g.17346144C>T	GRCh38
NC_000010.10:g.17388143C>T , CM000672.1:g.17388143C>T	GRCh37
NC_000010.9:g.17428149C>T	NCBI36
NG_051597.1:g.114823G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377602.5:c.377+13370G>A MANE Select	ENSP00000366827.4:n.377+13370G>A
ENST00000648997.1:c.387+13370G>A
ENST00000377602.4:c.377+13370G>A	ENSP00000366827.4:n.377+13370G>A
NM_001004470.1:c.377+13370G>A	NP_001004470.1:n.377+13370G>A
XR_242697.2:n.503+13370G>A
NM_001004470.2:c.377+13370G>A	NP_001004470.1:n.377+13370G>A
NM_001345961.1:c.-77+13370G>A	NP_001332890.1:n.-77+13370G>A
NR_144322.1:n.509+13370G>A
XM_017016174.1:c.287+13370G>A	XP_016871663.1:n.287+13370G>A
XM_024447974.1:c.-77+13370G>A	XP_024303742.1:n.-77+13370G>A
XM_024447975.1:c.-77+13370G>A	XP_024303743.1:n.-77+13370G>A
XM_024447976.1:c.-77+13370G>A	XP_024303744.1:n.-77+13370G>A
XM_024447977.1:c.-77+13370G>A	XP_024303745.1:n.-77+13370G>A
XM_024447978.1:c.-77+13370G>A	XP_024303746.1:n.-77+13370G>A
NM_001004470.3:c.377+13370G>A MANE Select	NP_001004470.1:n.377+13370G>A
NM_001345961.2:c.-77+13370G>A	NP_001332890.1:n.-77+13370G>A
NR_144322.2:n.717+13370G>A